Osteogenesis Imperfecta, Type Xxii (OI22)

Alias:

Oi22

Osteogenesis Imperfecta, Iia 22

Osteogenesis Imperfecta 22

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Osteogenesis Imperfecta, Type Xxii, is also known as oi22. An important gene associated with Osteogenesis Imperfecta, Type Xxii is CCDC134 (Coiled-Coil Domain Containing 134). Affiliated tissues include bone and cortex, and related phenotypes are bowing of the long bones and short stature

Related ID：

MALACARDS：OST180

OMIM：619795

MESH：D010013